Evidence map›Paper›PMID 33288821›Full record

ArticleCommunications biology2020

Development of a penem antibiotic against Mycobacteroides abscessus.

Hunter R Batchelder, Elizabeth Story-Roller, Evan P Lloyd, Amit Kaushik, Kristina M Bigelow, Emily C Maggioncalda, Eric L Nuermberger, Gyanu Lamichhane, Craig A Townsend

Open access · goldAbstract read
In one paragraph

Article in Communications biology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.9field-weighted citation impact, top 13% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

12 citing papers in PubMed, 19 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Review
  5. Article
  6. Article
  7. Article
  8. T405, a New Penem, ExhibitsAntimicrobial agents and chemotherapy · 2022
    Article
  9. Article
  10. Article
  11. Review
  12. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors at 1 institution in 1 country.

Hunter R BatchelderDepartment of Chemistry, Johns Hopkins University, Baltimore, MD, 21218, USA.ORCID 0000-0001-7367-5568
Elizabeth Story-RollerCenter for Tuberculosis Research, Division of Infectious Diseases, Johns Hopkins University School of Medicine, Baltimore, MD, 21287, USA.
Evan P LloydDepartment of Chemistry, Johns Hopkins University, Baltimore, MD, 21218, USA.ORCID 0000-0001-6984-7400
Amit KaushikCenter for Tuberculosis Research, Division of Infectious Diseases, Johns Hopkins University School of Medicine, Baltimore, MD, 21287, USA.ORCID 0000-0002-5622-1721
Kristina M BigelowCenter for Tuberculosis Research, Division of Infectious Diseases, Johns Hopkins University School of Medicine, Baltimore, MD, 21287, USA.
Emily C MaggioncaldaCenter for Tuberculosis Research, Division of Infectious Diseases, Johns Hopkins University School of Medicine, Baltimore, MD, 21287, USA.
Eric L NuermbergerCenter for Tuberculosis Research, Division of Infectious Diseases, Johns Hopkins University School of Medicine, Baltimore, MD, 21287, USA.
Gyanu LamichhaneCenter for Tuberculosis Research, Division of Infectious Diseases, Johns Hopkins University School of Medicine, Baltimore, MD, 21287, USA.ORCID 0000-0002-2214-0114
Craig A TownsendDepartment of Chemistry, Johns Hopkins University, Baltimore, MD, 21218, USA. ctownsend@jhu.edu.ORCID 0000-0003-2795-7585
Johns Hopkins University · US

Funding

Development of novel penems for drug-resistant tuberculosisR01AI137329 · NIAID · JOHNS HOPKINS UNIVERSITY · PI NUERMBERGER, ERIC L, TOWNSEND, CRAIG ARTHUR · 2018 to 2022
$3.9M
NIAID NIH HHS R01 AI137329
6 · The paper itself

Abstract

β-lactams are the most widely used antibiotic class to treat bacterial infections in humans. Mycobacteroides abscessus is an emerging pulmonary pathogen resistant to most antibiotics, including penicillins and cephalosporins. With no current FDA-approved treatment and cure rates <50%, there is a pressing need for effective therapies. Here we report T405, a new β-lactam of the penem subclass that exhibits potent activity against M. abscessus and a panel of drug-resistant strains isolated from cystic fibrosis patients. Additionally, in combination with the β-lactamase inhibitor avibactam, the rate of spontaneous resistance of M. abscessus to T405 approached the limit of detection. Lastly, we show the favorable pharmacokinetic profile of T405 in mice and the absence of toxicity at elevated dosage, which support the clinical potential of this compound.

Indexed as

AnimalsAnti-Bacterial Agentsbeta-LactamsDrug DesignDrug Resistance, BacterialHalf-LifeMiceMicrobial Sensitivity TestsMycobacterium abscessusAnti-Bacterial Agentsbeta-Lactams

Identifiers

PMID33288821
PMCPMC7721803
OpenAlexW3111659871

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.